Production : • To check the labels of raw material, packing materials and solvents before usage. • To maintain storage conditions of raw material/intermediates in plant. • To maintain process conditions for batch as per …
Skills: Production Monitoring, cGMP Compliance, Documentation, Safety Management, Equipment Calibration
Production : • To check the labels of raw material, packing materials and solvents before usage. • To maintain storage conditions of raw material/intermediates in plant. • To maintain process conditions for batch as per …
Skills: Production Monitoring, cGMP Compliance, Documentation, Safety Management, Equipment Calibration
Production : • To check the labels of raw material, packing materials and solvents before usage. • To maintain storage conditions of raw material/intermediates in plant. • To maintain process conditions for batch as per …
Skills: Production Monitoring, cGMP Compliance, Documentation, Equipment Calibration, Safety Management
Production : • To check the labels of raw material, packing materials and solvents before usage. • To maintain storage conditions of raw material/intermediates in plant. • To maintain process conditions for batch as per …
• To maintain and adherence of the GLP and safety procedures in laboratory. • To perform the analysis as per work allocation and records the results in work sheet (Protocols) for raw material / packing materials/intermed…
Skills: HPLC Analysis, GLP Compliance, CFR 21 Part 11, LIMS, Stability Study
Production : • To check the labels of raw material, packing materials and solvents before usage. • To maintain storage conditions of raw material/intermediates in plant. • To maintain process conditions for batch as per …
Skills: Production Monitoring, cGMP Compliance, Documentation, Equipment Calibration, Safety Management
Execute API manufacturing activities as per approved BMR, SOPs, and production plans. Supervise shift operations involving reactors, centrifuges, dryers, filters, and other process equipment. Ensure compliance with cGMP,…
Skills: API Manufacturing, cGMP Compliance, GDP, EHS, Data Integrity
Perform analysis of raw materials, intermediates, finished products, stability samples, and cleaning validation samples using HPLC, GC, UV-Visible Spectrophotometer, FTIR, Karl Fischer, Dissolution, and other laboratory …
Skills: HPLC, GC, UV-Visible Spectrophotometry, FTIR, Karl Fischer
Execute API manufacturing activities as per approved BMR, SOPs, and production plans. Supervise shift operations involving reactors, centrifuges, dryers, filters, and other process equipment. Ensure compliance with cGMP,…
Skills: API Manufacturing, cGMP Compliance, GDP, EHS, Data Integrity
• Work allocation for sampling , analysis related to microbial testing based on requirement and plan for sampling and analysis of finish products, & (test procedures and SOPs, and review of analysis data generated throug…
Monitor and maintain PLC, SCADA, and DCS-based process control systems. Diagnose and rectify control system failures in coordination with automation and production teams. Support modification, optimization, and commissio…
Skills: PLC, SCADA, DCS, Process Control Systems, Automation Systems
Execute API manufacturing activities as per approved BMR, SOPs, and production plans. Supervise shift operations involving reactors, centrifuges, dryers, filters, and other process equipment. Ensure compliance with cGMP,…
Skills: API Manufacturing, cGMP, GDP, EHS, Data Integrity
Perform analysis of raw materials, intermediates, finished products, in-process samples, solvents, and stability samples as per approved specifications and SOPs. Operate analytical instruments such as HPLC, GC, UV-Visibl…
Ensure compliance with cGMP, GDP, GLP, Data Integrity (ALCOA+), SOPs, and regulatory guidelines. Perform shop floor QA activities, including line clearance, equipment clearance, area clearance, and in-process verificatio…
Skills: cGMP, GDP, GLP, Data Integrity, Line Clearance
Production : • To check the labels of raw material, packing materials and solvents before usage. • To maintain storage conditions of raw material/intermediates in plant. • To maintain process conditions for batch as per …
Skills: Production Monitoring, cGMP Compliance, Documentation, Equipment Calibration, Safety Management
Execute manufacturing activities for API intermediates and finished active pharmaceutical ingredients as per approved Batch Manufacturing Records (BMRs), SOPs, and production plans. Operate and monitor process equipment …
Skills: API Manufacturing, cGMP Compliance, Good Documentation Practices, Process Equipment Operation, Line Clearance
JOB TITLE Assistant Manager- Quality Control, Chemistry REQUIREMENTS Education / Experience Post Graduate in Science (Organic or Analytical Chemistry ) 8 to 10 years in chemical & instrumental testing laboratory with exp…
Manage day-to-day operations of the QC laboratory, ensuring adherence to cGMP, GLP, and regulatory requirements. Review and approve analytical data, laboratory records, specifications, Certificates of Analysis (CoA), and…
• To maintain and adherence of the GLP and safety procedures in laboratory. • To perform the analysis as per work allocation and records the results in work sheet (Protocols) for raw material / packing materials/intermed…
Skills: HPLC Analysis, GLP Compliance, CFR 21 Part 11, LIMS, Stability Study
Execute batch manufacturing activities as per Batch Manufacturing Record (BMR), SOPs, and approved process parameters. Operate and monitor reactors, centrifuges, dryers, filters, blenders, and other process equipment. En…
Skills: Batch Manufacturing, cGMP, EHS, Data Integrity, Equipment Operation
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Full-time
Posted 5d ago
~40 hrs/week
Responsibilities
Responsible for overseeing production processes, maintaining batch records, and ensuring cGMP compliance in the finished powder processing section. The role involves supervising plant operators, managing equipment cleanliness, and coordinating with QC and Engineering departments.
Requirements
Requires proficiency in following BPRs and SOPs, managing plant utilities, and maintaining strict safety and environmental standards. Candidates must be able to handle chemical materials safely and maintain accurate technical documentation.
Full job description
Production
To check the labels of raw material, packing materials and solvents before usage.
To maintain storage conditions of raw material/intermediates in plant.
To maintain process conditions for batch as per BPRs.
To take instruction from shift Incharge/managers for batch charging / monitoring & follow up.
To report any deviation / discrepancy in plant / process to shift in charge.
To complete given task within stipulated time.
To maintain environment conditions in PP/Intermediate area as per SOP
To maintain reconciliation of accessories used in PP/Intermediate area.
To ensure that there is no any contamination in finished product
To do packing & repacking activities as per requirement
To follow proper entry & gowning procedure in PP/Intermediate area
To perform safe operations of plant equipments and utilities.
Documentation
To complete online BPR, equipment usage record & cleaning records with respect to his shift.
To fill area differential pressure record, centrifuge bags records and any other records related to PP area.
cGMP :
To guide & train workmen in Finished Powder Processing Section.
To ensure that yield & quality of finished product is as per predefined norms.
Packing of finished product is as per SOP.
Responsible for maintaining cleanliness of the equipments and area under his charge
To do proper calibrations of weighing balance, pH meter etc. as per SOP.
To update equipment status boards timely.
To ensure on line completion of equipment usage log.
To maintain proper labeling of HDPE / Fiber drums, hose pipes etc. used in respective batch processing.
To fill online documentation/BPR.
To participate in training to keep himself updated about cGMP, technical and safety standards and update his training records timely.
To maintain intermediate product & cleaning material reconciliation.
Safety
To keep himself aware about MSDS of related materials.
To educate and supervise plant operators in safe handling of chemicals and equipment so as to prevent accidents
To coordinate with EHS for various safety permits.
To use scrubber wherever required to avoid air pollution.
Wastage Avoidance / Reduction
To ensure no spillage of solvents & wastage of material.
To close the valves of utilities supplies when not required.
Inter departmental co-ordination
To coordinate with QC department for getting analysis report.
To coordinate with Engg Service for maintenance related work in his shift.
Founded by Shri I.A. Modi, Cadila Pharmaceuticals Ltd. is one of the largest privately held pharmaceutical companies in India, headquartered at Ahmedabad, in the State of Gujarat. Over the last seven decades, the company has been developing and manufacturing pharmaceutical products in India and selling and distributing these in over hundred other countries around the world.
Focused strongly on Innovation and Research, the company is present in more than forty-five therapeutic areas spread across twelve specialities, including cardiovascular, gastrointestinal, analgesics, haematinics, anti-infectives and antibiotics, respiratory agents, antidiabetics and immunologicals.
At Cadila Pharmaceuticals, Research and Development is at the core of all its initiatives, be it Biotechnology, APIs, Formulations, Plant Tissue Culture or Phytochemistry.
More than 300 scientists in its various Research and Development setups reinforce the competitiveness of research in the therapeutic areas which have high unmet medical needs.
Cadila Pharmaceuticals Excellence in manufacturing facilities is central to Cadila Pharmaceuticals. The company’s formulations manufacturing plant at Dholka near Ahmedabad, Gujarat is spread over hundred acres of land. This state-of-the- art facility is not only impressive in size, but is also USFDA approved.
The second formulations manufacturing facility is located at Samba in Jammu and Kashmir. The facility meets most of the stringent quality standards across the globe to produce tablets, capsules, soft and hard gelatin capsules, liquids and orals.
Two Active Pharmaceutical Ingredient (API) manufacturing units at Ankleshwar, Gujarat manufacture a wide range of APIs and intermediates including many USFDA-certified products.
The company has strong foothold in the African continent through its formulation manufacturing facility at Addis Ababa in Ethiopia.
For more information visit: https://www.cadilapharma.com/
How many Manufacturing jobs are open in Ankleshwar, India right now?
There are currently 165 open manufacturing positions in Ankleshwar, India listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Manufacturing roles in Ankleshwar, India?
Companies currently hiring include Cadila Pharmaceuticals Limited, Zentiva, Asian Paints, Indorama Ventures: Indovinya, among others. Browse the listings above to see every active employer.
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